570 likes | 2.22k Views
CONTROLLED HYPOTENSIVE ANAESTHESIA … what is safe ?. Dr Hussain Almejadi AL RAZI Hospital. Definition. History and evolution. Physiology. Blood pressure goal. Contraindications. Techniques. Anaesthetic management. Our experience in Al RAZI hospital. .
E N D
1. CONTROLLED HYPOTENSIVE ANAESTHESIAwhat is safe ? Dr Hussain Almejadi
AL RAZI Hospital
2. Definition.
History and evolution.
Physiology.
Blood pressure goal.
Contraindications.
Techniques.
Anaesthetic management.
Our experience in Al RAZI hospital.
3. why should we be bothered with hypotensive anaesthesia ?
Decrease blood loss.
Improve operative field.
Decrease duration of surgery.
4.
Decrease in blood loss by 55 % and shorten the operating time by one hour .
. Sum DC, Chung PC, Chen WC: Deliberate hypotensive anesthesia with labetalol in reconstructive surgery for scoliosis. Acta Anaesthesiol Sin 1996 Dec;34(4):203-207
5.
Significant less blood loss and improving of the surgical field.
Precious DS, Splinter W, Bosco D: Induced hypotensive anesthesia for adolescent orthognathic surgery J Oral Maxillofac Surg 1996 Jun;54(6):680-683
6.
Intraoperative blood loss is 40% less.
Nelson CL, Fontenot HJ: Ten strategies to reduce blood loss in orthopedic surgery Am J Surg 1995, N6A (Suppl.), 170:64-68
7. Deliberate hypotension in orthopedic surgery reduces blood loss, a meta analysis of RCT.
CANADAIN JOURNAL OF ANESTHESIA 2007
McMaster ,Hamilton,Ontario.
17 ARTICLES.
CONCLUSION : Deliberate hypotension does reduce blood loss.
8. Definition It is a State of induced hypotension during anaesthesia to reduce bleeding and improve the surgical field adjusted to the patients age ,pre-operative blood pressure and past medical history.
9. Definition Effect VS Safety .
Reduction in systolic blood pressure to
80 -90 mmHg.
Decrease in MAP to 50-60 mmHg in normotensive patients.
Reduction in MAP by 30% of the baseline values.
10. History 1917 Harvey Cushing for neurosurgery.
1943 Kolhstaedt and Page on dogs arterial bleeding.
1946 Gardner arteriotomy.
1948 High spinal.
1951 High epidural.
1951 Enderby ganlion blockade .
1960 Murtagh halothane.
1962 Moraca sodium nitroprusside.
1967 Dimant pacemaker.
1978 Fahmy nitroglycerin.
1981 Zimpfer verapamil.
1982 Fukunaga adenosine .
11. Physiology Cerebral circulation.
Coronary circulation.
Renal circulation.
12. Cerebral Autoregulation
13. Cerebral Circulation PaCO2 .
PaO2.
Temperature.
Volatile agents.
Vasodilators.
14. Coronary Circulation Dependent on aortic diastolic blood pressure.
Myocardium extracts most of the oxygen delivered.
Circulation is autoregulated .
15. Renal Circulation Autoregulation over the range 80-180 mmHg ( Miles and Venton 1954 )
MAP less than 75 mmHg leads to decrease in GFR ( Larson et al, 1974 )
Opioids and inhalational agents stimulate ADH release (Stunn 1974 )
16. Respiratory System Increase in blood flow to the dependent areas.
Vasodilators inhibits hypoxic pulmonary vasoconstriction.
PaCO2 and EtCO2 gradient increase.
17. Blood Pressure Goal Reduce blood loss.
Improve the surgical field .
18. Contraindications Anaethetist factors.
Patients factors.
19. Anaesthetist factors Lack of understanding of the technique.
Lack of technical experience.
Inability to monitor the patient adequately.
20. Patient factors Cardiac disease .
Diabetes .
Anemia.
Hepatic disease.
Ischaemic cerebrovascular disease.
Renal disease.
Respiratory insufficiency.
Severe systemic hypertension.
Intolerance to drugs used for hypotensive anaesthesia.
21. Absolute contraindications Known drug allergy.
Inability to monitor the patient adequately.
Unfamiliarity with the technique.
22. Morbidity and Mortality 1954 little et al
mortality 1 in 291
morbidity 1 in 31.
Systolic pressure below 80 mmHg.
2008 karol et al Anaesthes and Anlgesia.
NO DIFFERENCE.
23. Techniques MAP = CO x SYSTEMIC VASCULAR RESISTANCE
24. Decrease cardiac output Reduce blood volume.
Dilate capacitance vessels.
Decrease cardiac contractility .
Decrease of heart rate.
25. Peripheral vascular resistance Blockade of alpha adrenergic receptors.
Blockade of autonomic ganglion.
Ralaxation of vascular smooth muscle.
26. Mechanical manoeuvers Positioning .
Positive airway pressure.
Spinal anesthesia.
Epidural anesthesia.
27. Pharmacologic technique
Ideal agent
- Ease of administration
- Predictable & dose-dependent effect
- Rapid onset/offset
- Quick elimination without the
production of toxic metabolites
- Minimal effects on blood flow to vital
organs
28. Inhalational anesthetics negative inotropic effect vasodilation
Advantage
Provides surgical anesthesia
Rapid onset/offset
Easy to titrate
Cerebral protection
Disadvantage
Decreases CO
Cerebral vasodilation
29. Sodium nitroprusside Direct vasodilator (nitric oxide release) Advantage
Rapid onset/offset
East to titrate
Increases CO Disadvantage
Cyanide/thiocyanate toxicity
Increased ICP
Increased pulm. shunt
Sympathetic stimulation
Rebound hypertension
Coronary steal
Tachycardia
30. Nitroglycerin Direct vasodilator (nitric oxide release) Advantage
Rapid onset/offset
East to titrate
Limited increase in heart rate
No coronary steal Disadvantage
Lack of efficacy-depending on anesthetic technique
Increased ICP
Increased pulm. shunt
Methemoglobinemia
Inhibition of plt. aggregation
31. Beta adrenergic antagonist Beta adrenergic blockade (decreased myocardial contractility) Advantage
Rapid onset/offset
Decreased myocardial O2 consumption
No increase in ICP
No increase in pulm. shunt Disadvantage
Decreased CO
Heart block
Bronchospasm
Limited efficacy when used alone
32. Calcium channel blocker - vasodilation Advantage
Rapid onset
Limited increase in HR
Increase CO
No effect on airway reactivity
Increased GFR/urine output Disadvantage
Prolonged duration of action
Increased ICP
Increased pulm. shunt
33. Remifentanil
Remifentanil is an OPIOID
Pure m agonist
little binding at k, s, and d receptors
Rapid onset/offset
Decreases blood pressure & heart rate
No need for additional use of a potent
hypotensive or adjunct agents
34. Remifentanil Key Concepts Remifentanil is an ESTER
. Metabolized by nonspecific esterases in blood and tissue
Anesthesia maintained with high-dose remifentanil will be associated with rapid recovery.
Within 5-10 minutes of turning off an infusion there is virtually no residual remifentanil drug effect
37. Dosing and Administration Dex. should be administered using a controlled infusion device.
Dex. dosing should be individualized and titrated to the desired clinical effect
For adult patients Dex. is generally initiated with a infusion of 1mcg/kg over 10 minutes, followed by a maintenance infusion of 0.2 to 0.7 mcg/kg/hr
It is not necessary to discontinue Dex. prior to extubation
38. Comparison between dexmedetomidine and remifentanil for controlled hypotension during tympanoplasty.
CONCLUSIONS: Infusion of dexmedetomidine, at the doses used in this study, was less effective than remifentanil in achieving controlled hypotension, good surgical field exposure condition and surgeons' satisfaction during tympanoplasty.
2008-05, Eur J Anaesthesiol., 25(5):369-74. Epub 2008 Feb 25.
39. Preoperative management Thorough knowledge by the anaesthetist.
Proper patient evaluation and selection.
HB of 10 g/dl.
Arterial blood gas analysis sampling.
Good level of anxiolytics ,analgesics .
Vagolytic drugs should be avoided.
40. Intraoperative management Stress free induction.
Nasal intubation ?.
Enough peripheral venous access.
Pressure points.
41. Monitoring Invasive blood pressure .
Invasive blood pressure.
ECG V5 lead with ST segment analysis.
Central venous pressure.
Urine output.
Temperature.
Blood loss.
42. Fluid therapy Deficit replacement.
Maintenance.
Blood loss.
43. Induced hypotension should start at the time of mucosal incision .
Only to the level needed to reduce bleeding.
Only during specific surgical phase.
44. Postoperative management Rebound hypertension.
Reactionary hemorrhage.
45. Our experience in AL RAZI hospital Strong points.
Area of improvement.
46. Strong points One OT is allocated for hypotensive anaesthesia/TIVA.
Propofol remifentenyl.
Invasive monitoring is a must.
47. Area of improvement Patients selection.
Reduction in blood transfusion.
48. Future studies Prospective.
Control of age and physical status.
Bigger sample size.
Type of surgery.
Controlled studies.
Same technique.
Doppler technique.
50. THANK YOU THANK YOU